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Identifying the water mass composition of a sample has never been so easy!

Posted by mmaheigan

· Thursday, August 31st, 2023

When we collect seawater in any point of the ocean, we are collecting a mix of water masses from different origin that traveled until there keeping their salinity and temperature properties. The Atlantic Ocean is likely the most complex basin in term of water masses containing more than 15 in its depths. Some of them were “born” in the North Atlantic Ocean, others in the Southern Ocean, even in the Mediterranean Sea! And when we collect a seawater sample we can know which water masses are there, where they come from, what happened to each of them during their journey to us, what story can they tell us.

The variation of any non-conservative property (such as dissolved organic carbon or nutrients) in the deep open ocean depends on the mixing of those water masses and on the biogeochemical processes affecting it (such as heterotrophic respiration). But the effect of the water mass mixing is usually very high, so in order to study the biogeochemical processes, it is necessary to remove that effect.

On the other hand, estimating the contribution of the water masses composing a sample is useful to trace the distribution of each water mass identifying the depth of maximum water mass contribution or the depth-range where the water mass is dominant contributing > 50%. Ocean biogeochemists and microbiologists can get more out of their data estimating the impact of water mass mixing on the variability of any chemical (e.g. inorganic nutrients and dissolved organic carbon) or biological (e.g. prokaryotic heterotrophic abundance and production) property.

Knowing the contribution of each water mass to each sample was not an easy task and required expertise on the origin, circulation and mixing patterns of the water masses present in the study area. This could be even harder in very complex oceanic basin such as the deep Atlantic Ocean. The most commonly used methodology is the Optimum Multi-Parameter (OMP) analysis that was first applied by Tomczak in 1981. However, this methodology is time consuming and requires availability of a large set of quality-controlled chemical variables (e.g. nutrients, oxygen,..) together with a deep knowledge of the oceanography of the studied area. Those chemical variables are not always available or do not have the required quality by contrast to potential temperature and salinity that are high standard core variables in any cruise or database. In a recent research article, we applied multi-regression machine learning models to solve ocean water mass mixing. The models tested were trained using the solutions from OMP analyses previously applied to samples from cruises in the Atlantic Ocean. Extremely Randomized Trees algorithm yielded the highest score (R² = 0.9931; mse = 0.000227). The model allows solving the mixing of water masses in the Atlantic Ocean using potential temperature, salinity, latitude, longitude and depth. Potential temperature and salinity are the most commonly collected and curated variables in oceanography both from oceanographic cruises and autonomous vehicles (e.g. ARGO) avoiding the use of less commonly measured chemical variables which also require longer and time-consuming analyses of both the water samples and the data.

Figure 1. A16 section for the contribution of the water masses (A) AAIW5, (B) ENACW12, (C) AAIW3, (D) MW, (E) LSW, (F) ISOW, (G) CDW and (H) WSDW obtained with the Extremely Randomized Trees algorithm. Ocean Data View software (Schlitzer, 2015).

We also provide the code with instructions where any user can easily introduce the required variables (latitude, longitude, depth, temperature and salinity) of the chosen Atlantic samples and obtain the water mass proportion of each one in a fast and easy way. Actually, it would allow the user to obtain this information in real time during a cruise.

New research using other methods like OMP and its variants can be incorporated to the existing model increasing its accuracy and prediction capacity. Help us to improve the model and increase its spatial resolution!

Ocean biogeochemists and microbiologists can benefit from this tool even if they do not have a deep knowledge of the oceanography of the studied area. Identifying the water masses composition of a sample has never been so easy!

Author
Cristina Romera-Castillo (Instituto de Ciencias del Mar-CSIC, Barcelona, Spain)

Twitter: @crisrcas

Hydrostatic pressure substantially reduces deep-sea microbial activity

Posted by mmaheigan

· Thursday, May 11th, 2023

Deep sea microbial communities are experiencing increasing hydrostatic pressure with depth. It is known that some deep sea microbes require high hydrostatic pressure for growth, but most measurements of deep-sea microbial activity have been performed under atmospheric pressure conditions.

In a recent paper published in Nature Geoscience, the authors used a new device coined ‘In Situ Microbial Incubator’ (ISMI) to determine prokaryotic heterotrophic activity under in situ conditions. They compared microbial activity in situ with activity under atmospheric pressure at 27 stations from 175 to 4000 m depths in the Atlantic, Pacific, and the Southern Ocean. The bulk of heterotrophic activity under in situ pressure is always lower than under atmospheric pressure conditions and is increasingly inhibited with increasing hydrostatic pressure. Single-cell analysis revealed that deep sea prokaryotic communities consist of a small fraction of pressure-loving (piezophilic) microbes while the vast majority is pressure-insensitive (piezotolerant). Surprisingly, the piezosensitive fraction (~10% of the total community) responds with a more than 100-fold increase of activity upon depressurization. In the microbe proteomes, the authors uncovered taxonomically characteristic survival strategies in meso- and bathypelagic waters. These findings indicate that the overall heterotrophic microbial activity in the deep sea is substantially lower than previously assumed, which implies major impacts on the carbon budget of the ocean’s interior.

Figure caption: Deep sea microbial activity under varying pressure. (a) In situ bulk leucine incorporation rates normalized to rates obtained at atmospheric pressure conditions. (b) A microscopic view of a 2000 m sample collected in the Atlantic and incubated under atmospheric pressure conditions. The black halos around the cells are silver grains corresponding to their activities. The highly active cells (indicated by arrows) were rarely found in in situ pressure incubations. (c) Depth-related changes in the metaproteome of three abundant deep sea bacterial taxa (Alteromonas, Bacteroidetes, and SAR202). The number indicates shared and unique up- and down-regulated proteins in different depth zones.

Authors
Chie Amano (University of Vienna, Austria)
Zihao Zhao (University of Vienna, Austria)
Eva Sintes (University of Vienna, IEO-CSIC, Spain)
Thomas Reinthaler (University of Vienna, Austria)
Julia Stefanschitz (University of Vienna, Austria)
Murat Kisadur (University of Vienna, Austria)
Motoo Utsumi (University of Tsukuba, Japan)
Gerhard J. Herndl (University of Vienna, Netherlands Institute for Sea Research)

Twitter @microbialoceanW

Severe warming = 15% increase in bacterial respiration: Southern Ocean most impacted

Posted by mmaheigan

· Thursday, March 30th, 2023

The utilization, respiration, and remineralization of organic matter exported from the ocean surface to its depths are key processes in the ocean carbon cycle. Marine heterotrophic Bacteria play a critical role in these activities. However, most three-dimensional (3-D) coupled physical-biogeochemical models do not explicitly include Bacteria as a state variable. Instead, they rely on parameterization to account for the bacteria’s impact on particle flux attenuation.

A recent study examined how bacteria respond to climate change by employing a 3-D coupled ocean biogeochemical model that incorporates explicit bacterial dynamics. The model (CMCC-ESM2) is a part of the Coupled Model Intercomparison Project Phase 6. The authors first evaluated the reliability of century-scale forecasts (2015-2099) for bacterial stocks and rates in the upper 100 m layer against the compiled measurements from the contemporary period (1988-2011). Next the authors analyzed the predicted trends in bacterial stocks and rates under diverse climate scenarios and explored their association with regional differences in temperature and organic carbon stocks. Three crucial findings were revealed. There is a global-scale decrease in bacterial biomass of 5-10%, with a 3-5% increase in the Southern Ocean (Figure 1). In the Southern Ocean, the rise in semi-labile dissolved organic carbon (DOC) leads to an increase in DOC uptake rates of free-living bacteria; in the northern high and low latitudes, the increase in temperature drives the increase in their DOC uptake rates. Importantly, extreme warming could result in a global increase (up to 15%) and even higher in the Southern Ocean (21% increase) in bacterial respiration (Figure 1), potentially leading to a decline in the biological carbon pump.

This analysis is an unprecedented and early effort to understand the climate-induced changes in bacterial dynamics on a global scale in a systematic manner. This study takes us one step closer to comprehending how bacteria influence the functioning of the biological carbon pump and the distribution of organic carbon pools between surface and deep layers, especially their response to climate change.

Figure 1. Global projections of bacterial carbon stocks and rates during the baseline period (1990-2013) and their changes as anomalies under the most-severe climate change scenario (i.e., SSP5-8.5) relative to the baseline period (2076-2099). The stocks and rates during the baseline period (a, b, c, g, h, i) and their changes as anomalies under the most-severe climate change scenario (d, e, f, j, k, l). All variables are depth-integrated in the upper 100 m. Solid-line contours as standard deviation from averaging over 1990-2013. Anomalies are 2076-2099 average values relative to 1990-2013 average values. Global bacterial biomass has decreased by 5-10%, with a 3-5% increase in the Southern Ocean. However, extreme warming may increase bacterial respiration worldwide, thereby reducing the efficiency of the biological carbon pump. This study provides an early attempt to understand the response of bacteria to climate change and their impact on the distribution of organic carbon in the ocean.

Author
Heather Kim, Woods Hole Oceanographic Institution

An expanding understanding of Southern Ocean productivity and export

Posted by mmaheigan

· Monday, February 13th, 2023

Biology in the Southern Ocean is known to help regulate Earth’s climate by capturing and eventually sequestering carbon from its surface. Unfortunately, accurate estimates of the magnitude of the Southern Ocean (SO) biological carbon sink are limited and subject to ongoing debate. However, a recently published study used the expanding Southern Ocean BGC-Argo fleet to provide new estimates of SO Annual Net Community Production (ANCP) and export production.

Over long enough time and space scales (>1000 km and seasons), ANCP is equal to the amount of carbon fixed during photosynthesis that is not remineralized in the surface layer. What remains is available to be exported to depth. As this organic matter sinks out of the surface ocean, most of it is eventually remineralized by bacteria, leaving behind a signature of depleted oxygen. With enough floats, basin-scale ANCP can be estimated from the seasonal oxygen drawdown measured across their profiles. While similar studies have been carried out on single floats, here, the authors construct a composite of all available profiles and include a greater depth range than previously considered.

Figure 1. All available BGC-ARGO float profiles (25,512) were used to create an A) ensemble seasonal cycle in surface chlorophyll and sub-surface oxygen. B) Annual Net Community Production (ANCP) was then estimated by computing the depth-integrated oxygen depletion during the productive period. C) ANCP was estimated across 12 major regions, separated by the Indian, Pacific and Atlantic basins and Subantarctic (SAZ), Polar (PFZ), Antarctic (AZ), and Southern (S) frontal zones. Each region used 100s-1000s of individual float profiles (color-coded scatter points).

Results from this novel approach estimate SO ANCP (and ~export) at 3.89 GT C year^-1, with basin-scale regional estimates as much as a factor 2.8 larger than previous studies. Moreover, nearly 30% of remineralization was measured at depths not typically considered, with 14% below 500 m and another 15% immediately below the euphotic depth but above 100 m. These values suggest a more critical role for the Southern Ocean in regulating oceanic carbon storage, atmospheric CO₂ exchange, and climate than previously thought.

Authors:
Jiaoyang Su (University of Tasmania, Australia)
Christina Schallenberg (University of Tasmania, and Australian Antarctic Program Partnership)
Tyler Rohr (Australian Antarctic Program Partnership)
Peter G. Strutton (University of Tasmania, Australia)
Helen E. Phillips (University of Tasmania, and Australian Antarctic Program Partnership)

Integrated analysis of carbon dioxide and oxygen concentrations as a quality control of ocean float data

Posted by mmaheigan

· Friday, August 26th, 2022

A recent study in Communications Earth & Environment, examined spatiotemporal patterns of the two dissolved gases CO₂ and O₂in the surface ocean, using the high-quality global dataset GLODAPv2.2020. We used surface ocean data from GLODAP to make plots of carbon dioxide and oxygen relative to saturation (CORS plots). These plots of CO₂ deviations from saturation (ΔCO₂) against oxygen deviations from saturation (ΔO₂) (Figure 1) provide detailed insight into the identity and intensity of biogeochemical processes operating in different basins.

Figure 1: Relationships between ΔCO₂ and ΔO₂ in the global ocean basins based on surface data in the GLODAPv2.2020 database. The black dashed lines are the least-squares best-fit lines to the data; unc denotes the uncertainty in the y-intercept value with 95% confidence; r is the associated Pearson correlation coefficient; n is the number of data points.

In addition, data in all basins and all seasons shares some common behaviors: (1) negative slopes of best fit lines to the data, and (2) near-zero y-intercepts of those lines. We utilized these findings to compare patterns in CORS plots from GLODAP with those from BGC-Argo float data from the Southern Ocean Carbon and Climate Observations and Modeling (SOCCOM) program. Given that the float O₂ data is likely to be more accurate than the float pH data (from which the float CO₂ is calculated), CORS plots are useful for detecting questionable float CO₂ data, by comparing trends in float CORS plots (e.g. Figure 2) to trends in GLODAP CORS plots (Figure 1). As well as the immediately detected erroneous data, we discovered significant discrepancies in ΔCO₂-ΔO₂ y-intercepts compared to the global reference (i.e., GLODAPv2.2020 y-intercepts, Figure 1). The y-intercepts of 48 floats with QCed O₂ and CO₂ data (at regions south of 55°S) were on average greater by 0.36 μmol kg⁻¹ than the GLODAP-derived ones, implying the overestimations of float-based CO₂ release in the Southern Ocean.

Figure 2. CORS plots from data collected by SOCCOM floats F9096 and F9099 in the high-latitude Southern Ocean. Circles with solid edges denote data flagged as ‘good’, whereas crosses denote data flagged as ‘questionable’.

Our study demonstrates CORS plots’ ability to identify questionable data (data shown to be questionable by other QC methods) and to reveal issues with supposed ‘good’ data (i.e., quality issues not picked up by other QC methods). CORS plots use only surface data, hence this QC method complements existing methods based on analysis of deep data. As the oceanographic community becomes increasingly reliant on data collected from autonomous platforms, techniques like CORS will help diagnose data quality, and immediately detect questionable data.

Authors:
Yingxu Wu (Polar and Marine Research Institute, Jimei University, Xiamen, China; University of Southampton)
Dorothee C.E. Bakker (University of East Anglia)
Eric P. Achterberg (GEOMAR Helmholtz Centre for Ocean Research Kiel)
Amavi N. Silva (University of Southampton)
Daisy D. Pickup (University of Southampton)
Xiang Li (George Washington University)
Sue Hartman (National Oceanography Centre, Southampton)
David Stappard (University of Southampton)
Di Qi (Polar and Marine Research Institute, Jimei University, Xiamen, China)
Toby Tyrrell (University of Southampton)

How does the competition between phytoplankton and bacteria for iron alter ocean biogeochemical cycles?

Posted by mmaheigan

· Friday, August 26th, 2022

Free-living bacteria play a key role in cycling essential biogeochemical resources in the ocean, including iron, via their uptake, transformation, and release of organic matter throughout the water column. Bacteria process half of the ocean’s primary production, remineralize dissolved organic matter, and re-direct otherwise lost organic matter to higher trophic levels. For these reasons, it is crucial to understand what factors limit the growth of bacteria and how bacteria activities impact global ocean biogeochemical cycles.

In a recent study, Pham and colleagues used a global ocean ecosystem model to dive into how iron limits the growth of free-living marine bacteria, how bacteria modulate ocean iron cycling, and the consequences to marine ecosystems of the competition between bacteria and phytoplankton for iron.

Figure 1: (a) Iron limitation status of bacteria in December, January, and February (DJF) in the surface ocean. Low values (in blue color = close to zero) mean that iron is the limiting factor for the growth of bacteria; (b) Bacterial iron consumption in the upper 120m of the ocean and (c) Changes (anomalies) in export carbon production when bacteria have a high requirement for iron.

Through a series of computer simulations performed in the global ocean ecosystem model, the authors found that iron is a limiting factor for bacterial growth in iron-limited regions in the Southern Ocean, the tropical, and the subarctic Pacific due to the high iron requirement and iron uptake capability of bacteria. Bacteria act as an iron sink in the upper ocean due to their significant iron consumption, a rate comparable to phytoplankton. The competition between bacteria and phytoplankton for iron alters phytoplankton bloom dynamics, ocean carbon export, and the availability of dissolved organic carbon needed for bacterial growth. These results suggest that earth system models that omit bacteria ignore an important organism modulating biogeochemical responses of the ocean to future changes.

Authors:
Anh Le-Duy Pham (Laboratoire d’Océanographie et de Climatologie: Expérimentation et Approches Numériques (LOCEAN), IPSL, CNRS/UPMC/IRD/MNHN, Paris, France)
Olivier Aumont (Laboratoire d’Océanographie et de Climatologie: Expérimentation et Approches Numériques (LOCEAN), IPSL, CNRS/UPMC/IRD/MNHN, Paris, France)
Lavenia Ratnarajah (University of Liverpool, United Kingdom)
Alessandro Tagliabue (University of Liverpool, United Kingdom)

Ice sheets mobilize trace elements for export downstream

Posted by mmaheigan

· Thursday, January 7th, 2021

Trace elements are essential micronutrients for life in the ocean and also serve as valuable fingerprints of chemical weathering. The behaviour of trace elements in the ocean has gained interest because some of these elements are found at vanishingly low concentrations that limit ecosystem productivity. Despite delivering >2000 km³ yr^-1 of freshwater to the polar oceans, ice sheets have largely been overlooked as major trace element sources. This is partly due to a lack of data on meltwater endmember chemistry beneath and emerging from the Greenland and Antarctic ice sheets, which cover 10% of Earth’s land surface area, and partly because meltwaters were previously assumed to be dilute compared to most river waters.

In a study published in PNAS, authors analysed the trace element composition of meltwaters from the Mercer Subglacial Lake, a hydrologically active subglacial lake >1000 m below the surface of the Antarctic Ice Sheet, and a meltwater river emerging from beneath a large outlet glacier of the Greenland Ice Sheet (Leverett Glacier). These subglacial meltwaters (i.e., water travelling along the ice-rock interface beneath an ice mass) contained much higher concentrations of trace elements than anticipated. For example, typically immobile elements like iron and aluminium were observed in the dissolved phase (<0.45 µm) at much higher concentrations than in mean river or open ocean waters (up to 20,900 nM for Fe and 69,100 nM for Al), but exhibited large size fractionation between colloidal/nanoparticulate (0.02 – 0.45 µm) and soluble (<0.02 µm) size fractions (Figure 1). Subglacial physical and biogeochemical weathering processes are thought to mobilize many of these trace elements from the bedrock and sediments beneath ice sheets and export them downstream. Antarctic subglacial meltwaters were more enriched in dissolved trace elements than Greenland Ice Sheet outflow, which is likely due to longer subglacial residence times, lack of dilution from surface meltwater inputs, and differences in underlying sediment geology.

These results indicate that ice sheet systems can mobilize large quantities of trace elements from the land to the ocean and serve as major contributors to regional elemental cycles (e.g., coastal Southern Ocean). In a warming climate with increasing ice sheet runoff, subglacial meltwaters will become an increasingly dynamic source of micronutrients to coastal oceanic ecosystems in the polar regions.

Figure caption: Leverett Glacier (Greenland Ice Sheet) and Mercer Subglacial Lake (Antarctic Ice Sheet) dissolved elemental concentrations (<0.45 µm) normalized to mean non-glacial riverine trace element concentrations (Gaillardet et al., 2014) and major element concentrations (Martin and Meybeck, 1979). Grey regions indicate ±50 % of the riverine mean. Although major elements can be significantly depleted compared to non-glacial rivers, trace elements are commonly similar to or enriched.

Authors:
Jon R. Hawkings (Florida State Univ and German Research Centre for Geosciences)
Mark L. Skidmore (Montana State Univ)
Jemma L. Wadham (Univ of Bristol, UK)
John C. Priscu (Montana State Univ)
Peter L. Morton (Florida State Univ)
Jade E. Hatton (Univ of Bristol, UK)
Christopher B. Gardner (Ohio State Univ)
Tyler J. Kohler (École Polytechnique Fédérale de Lausanne, Switzerland)
Marek Stibal (Charles University, Prague, Czech Republic)
Elizabeth A. Bagshaw (Cardiff Univ, UK)
August Steigmeyer (Montana State Univ)
Joel Barker (Univ of Minnesota)
John E. Dore (Montana State Univ)
W. Berry Lyons (Ohio State Univ)
Martyn Tranter (Univ of Bristol, UK)
Robert G. M. Spencer (Florida State Univ)
SALSA Science Team

How zooplankton control carbon export in the Southern Ocean

Posted by mmaheigan

· Thursday, December 3rd, 2020

The Southern Ocean exhibits an inverse relationship between surface primary production and export flux out of the euphotic zone. The causes of this production-export decoupling are still under debate. A recently published mini review in Frontiers in Marine Science focused on zooplankton, an important component of Southern Ocean food webs and the biological pump. The authors compared carbon export regimes from the naturally iron-fertilised Kerguelen Plateau (high surface production, but generally low export) with the iron-limited and less productive high nutrient, low chlorophyll (HNLC) waters south of Australia, where carbon export is relatively high.

Figure 1: The role of zooplankton in establishing the characteristic export regimes at two sites in the Southern Ocean, (a) the highly productive northern Kerguelen Plateau, which exhibits low export, and (b) the iron-limited waters south of Australia with low production, but relatively high carbon export.

Size structure and zooplankton grazing pressure are found to shape carbon export at both sites. On the Kerguelen Plateau, a large size spectrum of zooplankton acts as “gate-keeper” to the mesopelagic by significantly reducing the sinking flux of phytoaggregates, which establishes the characteristic low export regime. In the HNLC waters, however, the zooplankton community is low in biomass and grazes predominantly on smaller particles, which leaves the larger particles for export and leads to relatively high export flux.

Gaps in knowledge related to insufficient seasonal data coverage, understudied carbon flux pathways, and associated mesopelagic processes limit our current understanding of carbon transfer through the water column and export. More integrated data collection efforts, including the use of autonomous profiling floats (e.g., BGC-Argo), stationary moorings, etc., will improve seasonal carbon flux data coverage, thus enabling more reliable estimation of carbon export and storage in the Southern Ocean and improved projection of future changes in carbon uptake and atmospheric carbon dioxide levels.

Authors:
Svenja Halfter (University of Tasmania)
Emma Cavan (Imperial College London)
Ruth Eriksen (CSIRO)
Kerrie Swadling (University of Tasmania)
Philip Boyd (University of Tasmania)

Profiling floats reveal fate of Southern Ocean phytoplankton stocks

Posted by mmaheigan

· Tuesday, September 1st, 2020

More observations are needed to constrain the relative roles of physical (advection), biogeochemical (downward export), and ecological (grazing and biological losses) processes in driving the fate of phytoplankton blooms in Southern Ocean waters. In a recent paper published in Nature Communications, authors used seven Biogeochemical Argo (BGC-Argo) floats that vertically profiled the upper ocean every ten days as they drifted for three years across the remote Sea Ice Zone of the Southern Ocean. Using the floats’ biogeochemical sensors (chlorophyll, nitrate, and backscattering) and regional ratios of nitrate consumption:chlorophyll synthesis, the authors developed a new approach to remotely estimate the fate of the phytoplankton stocks, enabling calculations of herbivory and of downward carbon export. The study revealed that the major fate of phytoplankton biomass in this region is grazing, which consumes ~90% of stocks. The remaining 10% is exported to depth. This pattern was consistent throughout the entire sea ice zone where the floats drifted, from 60°-69° South.

Figure Caption: Southern Ocean Chlorophyll a climatology and floats’ trajectories (top panel). Total losses of Chlorophyll a (including grazing and phytodetritus export, left panel). Phytodetritus export (right panel).

This study region comprises two of the three major krill growth and development areas—the eastern Weddell and King Haakon VII Seas and Prydz Bay and the Kerguelen Plateau—so the observed grazing was probably due to Antarctic krill, underscoring their pivotal importance in this ecosystem. Building upon the greater understanding of ocean ecosystems via satellite ocean colour development in the 1990s, BGC-Argo floats and this new approach will allow remote monitoring of the different fates of phytoplankton stocks and insights into the status of the ecosystem.

Authors:
Sebastien Moreau (Norwegian Polar Institute, Tromsø, Norway)
Philip Boyd (Institute for Marine and Antarctic Studies, Hobart, Australia)
Peter Strutton (Institute for Marine and Antarctic Studies, Hobart, Australia)

A close-up view of biomass controls in Southern Ocean eddies

Posted by mmaheigan

· Thursday, August 20th, 2020

Southern Ocean biological productivity is instrumental in regulating the global carbon cycle. Previous correlative studies associated widespread mesoscale activity with anomalous chlorophyll levels. However, eddies simultaneously modify both the physical and biogeochemical environments via several competing pathways, making it difficult to discern which mechanisms are responsible for the observed biological anomalies within them. Two recently published papers track Southern Ocean eddies in a global, eddy-resolving, 3-D ocean simulation. By closely examining eddy-induced perturbations to phytoplankton populations, the authors are able to explicitly link eddies to co-located biological anomalies through an underlying mechanistic framework.

Figure caption: Simulated Southern Ocean eddies modify phytoplankton division rates in different directions of depending on the polarity of the eddy and background seasonal conditions. During summer anticyclones (top right panel) deliver extra iron from depth via eddy-induced Ekman pumping and fuel faster phytoplankton division rates. During winter (bottom right panel) the extra iron supply is eclipsed by deeper mixed layer depths and elevated light limitation resulting in slower division rates. The opposite occurs in cyclones.

In the first paper, the authors observe that eddies primarily affect phytoplankton division rates by modifying the supply of iron via eddy-induced Ekman pumping. This results in elevated iron and faster phytoplankton division rates in anticyclones throughout most of the year. However, during deep mixing winter periods, exacerbated light stress driven by anomalously deep mixing in anticyclones can dominate elevated iron and drive division rates down. The opposite response occurs in cyclones.

The second paper tracks how eddy-modified division rates combine with eddy-modified loss rates and physical transport to produce anomalous biomass accumulation. The biomass anomaly is highly variable, but can exhibit an intense seasonal cycle, in which cyclones and anticyclones consistently modify biomass in different directions. This cycle is most apparent in the South Pacific sector of the Antarctic Circumpolar Current, a deep mixing region where the largest biomass anomalies are driven by biological mechanisms rather than lateral transport mechanisms such as eddy stirring or propagation.

It is important to remember that the correlation between chlorophyll and eddy activity observable from space can result from a variety of physical and biological mechanisms. Understanding the nuances of how these mechanisms change regionally and seasonally is integral in both scaling up local observations and parameterizing coarser, non-eddy resolving general circulation models with embedded biogeochemistry.

Authors:
Tyler Rohr (Australian Antarctic Partnership Program, previously at MIT/WHOI)
Cheryl Harrison (University of Texas Rio Grande Valley)
Matthew Long (National Center for Atmospheric Research)
Peter Gaube (University of Washington)
Scott Doney (University of Virginia)

Funding for the Ocean Carbon & Biogeochemistry Project Office is provided by the National Science Foundation (NSF) and the National Aeronautics and Space Administration (NASA). The OCB Project Office is housed at the Woods Hole Oceanographic Institution.

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